89224-73-7

Basic information

• Product Name: 4H-Furo[3,2-b]indole-2-carboxamide, 3,7-dimethoxy-4-phenyl-
• CAS NO: 89224-73-7
• Molecular Formula: C19H16N2O4
• Molecular Weight: 336.347
• Mol File: 89224-73-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4H-Furo[3,2-b]indole-2-carboxamide, 3,7-dimethoxy-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-Furo[3,2-b]indole-2-carboxamide, 3,7-dimethoxy-4-phenyl-(89224-73-7)
• EPA Substance Registry System: 4H-Furo[3,2-b]indole-2-carboxamide, 3,7-dimethoxy-4-phenyl-(89224-73-7)

Safety Data

• Hazardous Substances Data: 89224-73-7(Hazardous Substances Data)

Upstream product

• 89224-54-4 3,7-dimethoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 89224-79-3 5-methoxy-2-<(2-methoxy-2-oxoethyl)phenylamino>benzoic acid methyl ester 
• 89224-52-2 5-methoxy-3-(2-methoxy-2-oxoethoxy)-1-phenyl-1H-indole-2-carboxylic acid methyl ester 
• 93424-83-0 3-hydroxy-7-methoxy-4-phenyl-4H-furo<3,2-b>indole-2-carboxylic acid methyl ester 
• 89224-77-1 2-[(Cyanomethyl)phenylamino]-5-methoxy-benzoic acid 
• 89224-78-2 2-<(carboxymethyl)phenylamino>-5-methoxybenzoic acid 
• 89224-94-2 3-hydroxy-5-methoxy-1-phenyl-1H-indole-2-carboxylic acid methyl ester 
• 89224-76-0 6-methoxy-1-phenyl-1,2-dihydro-(4H)-3,1-benzoxazin-4-one 
• 89224-95-3 5-methoxy-2-(phenylamino)benzoic acid 

Downstream Products

• 89224-75-9 3,7-Dimethoxy-4-phenyl-2-(1H-tetrazol-5-yl)-4H-furo[3,2-b]indole 
• 89224-74-8 3,7-dimethoxy-4-phenyl-4H-furo[3,2-b]indole-2-carbonitrile 

Relevant articles and documents

Tetrazolyl- and carboxamidotetrazolyl-substituted 4H-furo[3,2-b] indoles and anti-allergic use thereof

Novel tetrazolyl- and carboxamidotetrazolyl-substituted 4H-furo[3,2-b] indoles are useful for treating allergies or for treating or ameliorating postmyocardial infarct tissue damage. Also disclosed are methods for preparing said indoles, pharmaceutical compositions containing said indoles and methods for using said pharmaceutical compositions.

Indole Esters as Heterocyclic Synthons. III . Preparation and Reactions of Furoindoles

The preparation of furoindoles via Dieckmann cyclization is described.The precursor diesters were obtained from 3-hydroxy-1H-indole-2-carboxylic acid esters and methyl or ethyl bromoacetate.Reactions of the furoindole enolic esters prepared